(Q8041552)

English

X-linked congenital stationary night blindness

medical condition

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Statements

0 references

1 reference

Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region

subclass of

congenital stationary night blindness

0 references

0 references

0 references

1 reference

Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity

CACNA1F

1 reference

stated in

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

Identifiers

MedlinePlus ID

003039

1 reference

imported from Wikimedia project

English Wikipedia

DiseasesDB

32689

1 reference

imported from Wikimedia project

0 references

1 reference

imported from Wikimedia project

English Wikipedia

ICD-9 ID

368.61

1 reference

imported from Wikimedia project

English Wikipedia

Medical Dictionary for Regulatory Activities ID

10029404

1 reference

reference URL

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

Microsoft Academic ID

2780096930

0 references

OMIM ID

310500

1 reference

imported from Wikimedia project

English Wikipedia

300071

1 reference

imported from Wikimedia project

English Wikipedia

Sitelinks

Wikipedia(6 entries)

arwiki العمى الليلي الثابت الخلقي
bswiki Urođeno stacionarno noćno sljepilo
dewiki Kongenitale stationäre Nachtblindheit
enwiki Congenital stationary night blindness
eswiki Ceguera nocturna estacionaria congénita autosómica recesiva
frwiki Cécité nocturne congénitale stationnaire

(Q8041552)

X-linked congenital stationary night blindness

Statements

Identifiers

Sitelinks

Wikipedia(6 entries)

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